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Corinne Collet

Showing results (31-40 of 93) with videos related to

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Clinical Genetics|June 21, 2026
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the LiteratureWafaa Alharbi, Abdul A Peer-Zada, Abeer S Alaqidi, et al.
Molecular Genetics & Genomic Medicine|May 3, 2021
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3ACaroline Caetano da Silva, Manon Ricquebourg, Philippe Orcel, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
Decreased osteoclastogenesis in serotonin-deficient miceYasmine Chabbi-Achengli, Amélie E Coudert, Jacques Callebert, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 8, 2010
Crouzon syndrome with acanthosis nigricans: a case-based updateFederico Di Rocco, Corinne Collet, Laurence Legeai-Mallet, et al.
European Journal of Oral Sciences|January 17, 2012
Enamel alterations in serotonin 2B receptor knockout miceYassine Harichane, Sasha Dimitrova-Nakov, Arnaud Marchadier, et al.
American Journal of Medical Genetics. Part A|August 30, 2014
Prenatal findings in carpenter syndrome and a novel mutation in RAB23Damien Haye, Corinne Collet, Catherine Sembely-Taveau, et al.
Bone Reports|April 4, 2022
Growth charts in <i>FGFR2</i>- and <i>FGFR3</i>-related faciocraniosynostosesCaroline Ea, Quentin Hennocq, Arnaud Picard, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 17, 2013
Differentially expressed genes in autosomal dominant osteopetrosis type II osteoclasts reveal known and novel pathways for osteoclast biologyAmélie E Coudert, Andrea Del Fattore, Céline Baulard, et al.
JHEP Reports : Innovation in Hepatology|September 22, 2025
Relative exchangeable copper: A highly specific and sensitive biomarker for Wilson disease diagnosisNouzha Djebrani-Oussedik, Clément Desjardins, Mickaël Alexandre Obadia, et al.
Bone|July 3, 2024
Evaluation of bone density and microarchitecture in adult patients with X-linked hypophosphatemic rickets: A pilot longitudinal studyThomas Funck-Brentano, Arnaud Vanjak, Agnes Ostertag, et al.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
Clinical Genetics|June 21, 2026
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the LiteratureWafaa Alharbi, Abdul A Peer-Zada, Abeer S Alaqidi, et al.
Molecular Genetics & Genomic Medicine|May 3, 2021
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3ACaroline Caetano da Silva, Manon Ricquebourg, Philippe Orcel, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
Decreased osteoclastogenesis in serotonin-deficient miceYasmine Chabbi-Achengli, Amélie E Coudert, Jacques Callebert, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 8, 2010
Crouzon syndrome with acanthosis nigricans: a case-based updateFederico Di Rocco, Corinne Collet, Laurence Legeai-Mallet, et al.
European Journal of Oral Sciences|January 17, 2012
Enamel alterations in serotonin 2B receptor knockout miceYassine Harichane, Sasha Dimitrova-Nakov, Arnaud Marchadier, et al.
American Journal of Medical Genetics. Part A|August 30, 2014
Prenatal findings in carpenter syndrome and a novel mutation in RAB23Damien Haye, Corinne Collet, Catherine Sembely-Taveau, et al.
Bone Reports|April 4, 2022
Growth charts in <i>FGFR2</i>- and <i>FGFR3</i>-related faciocraniosynostosesCaroline Ea, Quentin Hennocq, Arnaud Picard, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 17, 2013
Differentially expressed genes in autosomal dominant osteopetrosis type II osteoclasts reveal known and novel pathways for osteoclast biologyAmélie E Coudert, Andrea Del Fattore, Céline Baulard, et al.
JHEP Reports : Innovation in Hepatology|September 22, 2025
Relative exchangeable copper: A highly specific and sensitive biomarker for Wilson disease diagnosisNouzha Djebrani-Oussedik, Clément Desjardins, Mickaël Alexandre Obadia, et al.
Bone|July 3, 2024
Evaluation of bone density and microarchitecture in adult patients with X-linked hypophosphatemic rickets: A pilot longitudinal studyThomas Funck-Brentano, Arnaud Vanjak, Agnes Ostertag, et al.
Pageof 10